Two class action lawsuits seek to force Philips to reimburse those with recalled DreamStation CPAP machines for the cost of replacing the devices, which contain sound abatement foam that can…
The JPML has been asked to consolidate all Philips DreamStation CPAP recall lawsuits before one judge for pretrial proceedings.
A class action lawsuit calls for Philips to refund and replace recalled DreamStation CPAP machines, and to provide medical monitoring for users who may have inhaled or ingested cancer-causing, toxic…
The FDA is urging consumers affected by the Philips CPAP and BiPAP recall to heed warnings about the risks of respiratory injuries linked to degrading sound abatement foam.
A recent Philips DreamStation CPAP recall is raising questions as to what role third party cleaning devices using ozone or ultraviolet radiation may have played in customer illnesses.
Philips has recalled nearly 4 million CPAP, mechanical ventilator, and other breathing assistance devices due to the presence of foam which could degrade and cause breathing problems or even cancer.
The FDA has loosened some restrictions on the use of mechanical ventilators in order to help U.S. hospitals combat the growing coronavirus pandemic.
The FDA is warning CPAP users not to try to clean their devices using ozone gas or UV light, as these methods are unapproved, untested, and potentially dangerous.
The findings of a new study indicate that CPAP machines do not decrease the risks of heart attack or death for those suffering from sleep apnea.
More truck drivers than expected suffer from sleep apnea, but long-term treatment can reduce their risk of accidents, according to the findings of an Italian study.
